rs587776644(T;T)

common in clinvar

Is a	genotype
of	rs587776644
Gene	SDHD, TIMM8B
Chromosome	11
Position	112,086,961
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(G;T)	6.2	Hereditary PGL/PCC Syndrome
(T;T)	0	common in clinvar